Primary Site >> Stomach Cancer
Gene >> LIMK1
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336180 |
| Start | 74120902:74120902(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782125431 |
| CDS Mutation | c.1634G>A |
| AA Mutation | p.Arg545Gln(p.R545Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000336180 |
| Start | 74096624:74096624(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.155G>A |
| AA Mutation | p.Cys52Tyr(p.C52Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336180 |
| Start | 74115839:74115839(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1448G>A |
| AA Mutation | p.Arg483His(p.R483H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000336180 |
| Start | 74099117:74099117(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.487G>A |
| AA Mutation | p.Val163Ile(p.V163I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336180 |
| Start | 74121268:74121268(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781901137 |
| CDS Mutation | c.1911C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336180 |
| Start | 74096628:74096628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.159T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000336180 |
| Start | 74115837:74115837(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782401601 |
| CDS Mutation | c.1446G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |